Literature DB >> 3022471

The primary structure of crossover regions of intertypic poliovirus recombinants: a model of recombination between RNA genomes.

L I Romanova, V M Blinov, E A Tolskaya, E G Viktorova, M S Kolesnikova, E A Guseva, V I Agol.   

Abstract

The nucleotide sequence of crossover sites in the genome of four intertypic (type 3/type 1) poliovirus recombinants has been determined. The approximate boundaries of the crossover regions were first estimated by RNase T1 oligonucleotide mapping of the recombinant genomes; then appropriate regions were sequenced by the chain termination method using oligonucleotide-primed reverse transcription of the recombinant RNAs. The crossover sites (defined as the contiguous sequences shared by the recombinant and both parental genomes flanked, in the recombinant genome, by heterotypic RNA segments) are 5, 5, 7, and 11 nucleotides long, respectively. The recombination was precise and was not accompanied by any other genetic alterations. The recombination sites were found to be located within genome segments having a potential to form secondary structure elements. Based on this observation, a model of recombination between picornaviral RNA genomes has been proposed. The essence of this model consists in bringing together homologous regions of two recombining RNA genomes via formation of intermolecular duplexes, detachment of the nascent 3' end of the newly synthesized complementary RNA from a "parting" site on the first template and its subsequent "jumping" to the identical (or closely related) "anchoring" site on the other template. Features of this model are discussed in some detail.

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Year:  1986        PMID: 3022471     DOI: 10.1016/0042-6822(86)90180-7

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  63 in total

1.  Frequent homologous recombination events between molecules of one RNA component in a multipartite RNA virus.

Authors:  A Bruyere; M Wantroba; S Flasinski; A Dzianott; J J Bujarski
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

2.  A human rotavirus with rearranged genes 7 and 11 encodes a modified NSP3 protein and suggests an additional mechanism for gene rearrangement.

Authors:  E Gault; N Schnepf; D Poncet; A Servant; S Teran; A Garbarg-Chenon
Journal:  J Virol       Date:  2001-08       Impact factor: 5.103

3.  Generation of coronavirus spike deletion variants by high-frequency recombination at regions of predicted RNA secondary structure.

Authors:  C L Rowe; J O Fleming; M J Nathan; J Y Sgro; A C Palmenberg; S C Baker
Journal:  J Virol       Date:  1997-08       Impact factor: 5.103

4.  Primer-dependent synthesis by poliovirus RNA-dependent RNA polymerase (3D(pol)).

Authors:  V Rodriguez-Wells; S J Plotch; J J DeStefano
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

5.  Recombination of poliovirus RNA proceeds in mixed replication complexes originating from distinct replication start sites.

Authors:  Denise Egger; Kurt Bienz
Journal:  J Virol       Date:  2002-11       Impact factor: 5.103

6.  Genetic recombination in brome mosaic virus: effect of sequence and replication of RNA on accumulation of recombinants.

Authors:  P D Nagy; J J Bujarski
Journal:  J Virol       Date:  1992-11       Impact factor: 5.103

7.  Nonreplicative homologous RNA recombination: promiscuous joining of RNA pieces?

Authors:  Anatoly P Gmyl; Sergey A Korshenko; Evegny V Belousov; Elena V Khitrina; Vadim I Agol
Journal:  RNA       Date:  2003-10       Impact factor: 4.942

8.  RNA recombination in vivo in the absence of viral replication.

Authors:  Andreas Gallei; Alexander Pankraz; Heinz-Jürgen Thiel; Paul Becher
Journal:  J Virol       Date:  2004-06       Impact factor: 5.103

9.  A model for rearrangements in RNA genomes.

Authors:  E V Pilipenko; A P Gmyl; V I Agol
Journal:  Nucleic Acids Res       Date:  1995-06-11       Impact factor: 16.971

10.  Hairpin structures are the primary amplification products: a novel mechanism for generation of inverted repeats during gene amplification.

Authors:  S Cohen; D Hassin; S Karby; S Lavi
Journal:  Mol Cell Biol       Date:  1994-12       Impact factor: 4.272

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